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GVHD, Chronic clinical trials

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NCT ID: NCT04930562 Completed - GVHD, Chronic Clinical Trials

Efficacy and Safety of BN101 in Subjects With Chronic Graft Versus Host Disease (cGVHD)

Start date: April 27, 2021
Phase: Phase 2
Study type: Interventional

This is a phase 2, open-label, multicenter trial to evaluate the efficacy and safety of BN101 in subjects with Chronic Graft Versus Host Disease (cGVHD) after at least First Line of systemic therapy.

NCT ID: NCT04884204 Completed - Clinical trials for Hematological Malignancy

Systematic Symptom Identification With Disease Specific PROM to Assess Symptoms of Chronic GVHD in Outpatient Care in Patients Post HSCT

SIMPly-CARE
Start date: April 30, 2021
Phase: N/A
Study type: Interventional

A two sited feasibility study to test the feasibility of systematic symptom identification with disease specific and clinically developed PROM (Lee Symptom Scale) longitudinally with a 12 month follow up in outpatient care in patients post HSCT to assess symptoms of chronic GVHD (n= 30).

NCT ID: NCT03042676 Completed - Acute Leukemia Clinical Trials

Electronic Database for the Follow up of the ATG_FamilyStudy

AFF
Start date: September 15, 2017
Phase:
Study type: Observational [Patient Registry]

Allogeneic hematopoietic stem cell transplantation (HSCT) is capable of definitive cure of acute leukemias. The most important post-transplant complication is graft vs host disease (GVHD) which can be substantially decreased by the addition of anti-T lymphocyte globulin (ATG-Grafalon) to the standard GVHD prophylaxis (cyclosporin and methotrexate) without any increase in relapses and infections (Kroger et al NEJM 2016, ClinicalTrials.gov number, NCT00678275). In the ATG_familystudy (prospective, randomised, multicenter study) a decrease in the incidence of chronic GVHD (from 67.8% to 32.2%) was observed after the addition of ATG (10 mg/kg for three days ,from day -3 to -1) to the standard GVHD prophylaxis in the setting of acute leukemias in any remission, receiving peripheral blood stem cells from an HLA identical sibling donor after myeloablative preparative regimen. In particular, the GVHD extensive form was reduced from 52.4% to 7.6%. The study has been closed in 2014 with a minimum follow up of 2 years from transplant. The investigators would like to evaluate the longer term follow up of this study.